HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 21634Generated: October 29, 2026
Benzoyl chloride → N'-t-butyl-N-phenylacetyl-N'-benzoylhydrazine
https://huagongshe.com/reaction/21634
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | Phenylacetyl chloride | HCID 7679 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | tert-Butylhydrazine monohydrochloride | HCID 81889 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | N'-t-butyl-N-phenylacetyl-N'-benzoylhydrazine | HCID 15451993 | — |
Reaction Steps
To a stirred suspension of t-butylhydrazine hydrochloride (2.0 g, 0.016M) in toluene (30 ml) was added 50% sodium hydroxide (1.3 g, 0.016M). After 15 minutes, the mixture was cooled to 5° C. and phenylacetyl chloride (2.4 g, 0.016M) and 50% sodium hydroxide (1.3 g, 0.016M) were added separately and simultaneously so as to maintain the reaction temperature below 10° C. After the addition, the reaction mixture was allowed to warm to room temperature and stirred for 1 hour. The mixture was diluted with hexane and the solid product isolated by filtration. This product (3.2 g, 0.015M) was dissolved in a stirred mixture of toluene (30 ml) and cooled on ice. To this mixture was added benzoylchloride (2.2 g, 0.016M) and 50% sodium hydroxide (1.3 g, 0.016M) simultaneously. After addition, the mixture was stirred for 1/2 hour, diluted with hexane and the solid product, N'-t-butyl-N-phenylacetyl-N'-benzoylhydrazine, isolated by filtration.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05424333 |
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| Source dataset | uspto-grants-1995_06 |
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| ORD ID | ord-5d4415c8f6eb4a69a72e4f28887b0d14 |
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| Source note | uspto-grants-1995_06 |
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